Involvement of aberrant miR-139/Jun feedback loop in human gastric cancer

Biochim Biophys Acta. 2015 Feb;1853(2):481-8. doi: 10.1016/j.bbamcr.2014.12.002. Epub 2014 Dec 10.

Abstract

Accumulating evidence indicates that some miRNAs could form feedback loops with their targets to fine-tune tissue homeostasis, while disruption of these loops constitutes an essential step towards human tumorigenesis. In this study, we report the identification of a novel negative feedback loop formed between miR-139 and its oncogenic target Jun. In this loop, miR-139 could inhibit Jun expression by targeting a conserved site on its 3'-UTR, whereas Jun could induce miR-139 expression in a dose dependent manner through a distant upstream regulatory element. Interestingly, aberration in this loop was found in human gastric cancer, where miR-139 was down-regulated and inversely correlated with Jun expression. Further functional analysis showed that restored expression of miR-139 in gastric cancer cells significantly induces apoptosis, and inhibits cell migration and proliferation as well as tumour growth through targeting Jun. Thus, our data strongly suggests a role of aberrant miR-139/Jun negative feedback loop in the development of human gastric cancer and miR-139 as a potential therapeutic target for gastric cancer. Given that miR-139 and Jun are deregulated in many cancers, our findings here might have broader implication in other types of human cancers.

Keywords: Feedback loop; Gastric cancer; Jun; MiR-139.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Carcinogenesis / genetics
  • Carcinogenesis / pathology
  • Cell Line, Tumor
  • Feedback, Physiological*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Molecular Sequence Data
  • Proto-Oncogene Proteins c-jun / metabolism*
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / pathology
  • Transcription, Genetic

Substances

  • MIRN139 microRNA, human
  • MicroRNAs
  • Proto-Oncogene Proteins c-jun